Optimizing feeding methods for preterm infants
Official title: How to Optimize Enteral Feeding of the Full Enteral Feeding Preterm Infant: Evaluation of Different Gastric Tube Management Practices
Run by IRCCS Azienda Ospedaliero-Universitaria di Bologna · NCT06760832 · Data updated 2026-11-12
This study is testing two different ways of feeding very low-birth-weight preterm infants to see which method helps them tolerate feeding better and have fewer problems.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna Academic / other |
| Locations | 1 site (Bologna, Bolgona) |
| Status | Recruiting |
| Started | July 21, 2020 |
| Main results expected | December 31, 2025 |
| Study ends | December 31, 2026 |
| Registry record updated | January 7, 2025 |
| Trial ID | NCT06760832 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are preterm infants born before 32 weeks of gestation or weighing less than 1500 grams who are receiving full enteral feeding.
✕Probably not a fit
Patients requiring invasive ventilatory support or those with congenital gastrointestinal malformations may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates different methods of enteral feeding in very low-birth-weight preterm infants who have achieved full enteral feeding. It compares intermittent gastric tube placement with permanent gastric tube maintenance to determine which method leads to better feeding tolerance and fewer adverse effects. The study will assess parameters such as gastric stagnation, cardio-respiratory events, and signs of discomfort related to tube management. The goal is to provide evidence-based recommendations for enteral feeding practices in this vulnerable population.
Why it matters
Potential benefit: If successful, this study could improve feeding tolerance and reduce adverse effects in preterm infants, enhancing their overall health outcomes.
How similar studies have gone: There is currently no literature directly comparing the different modes of enteral feeding management in preterm infants, making this approach novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Gestational Age \<32 weeks and/or neonatal weight \<1500 g * Achievement of full enteral feeding (150 ml/kg/day of milk) * Exclusive feeding of human milk (breast and/or bank) * Informed consent signed by parent or legal guardian Exclusion Criteria: * Need for invasive ventilatory support * Congenital malformations affecting the gastrointestinal tract
Where it's running
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IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, Bolgona, Italy Recruiting
Study contacts
- Principal investigator: Arianna Aceti, MD — IRCCS Azienda Ospedaliero-Universitaria di Bologna
- Study coordinator: Arianna Aceti, MD
- Email: arianna.aceti2@unibo.it
- Phone: 0512143779
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.